Job Summary
- Position: Trainee Technical Assistant (Production), QC Analyst (Chemical), and GLP Analyst (Chemical).
- Experience: Freshers (0 to 2 years) and Experienced Professionals (4 to 8 years).
- Location: Zydus Lifesciences Limited, Ahmedabad (Pharmez – SEZ).
- Walk-in Interview Date: 21st March 2026.
- Interview Time: 9:00 AM to 3:00 PM.
Company Overview
Zydus Lifesciences Limited (formerly known as Cadila Healthcare Limited) is a globally recognized pharmaceutical leader committed to improving lives through high-quality healthcare solutions. We are currently expanding our operations at our state-of-the-art Transdermal manufacturing facility in Ahmedabad. We are looking for talented, dedicated, and safety-conscious professionals to join our production and quality control teams.
Job Descriptions and Requirements
1. Trainee Technical Assistant (Production – Transdermal)
We are seeking entry-level candidates who are eager to launch their careers in the pharmaceutical manufacturing sector. This role is ideal for individuals who are detail-oriented and interested in working with sophisticated machinery.
- Qualifications: Diploma in Mechanical or Electrical engineering, or a D. Pharma degree.
- Experience: 0 to 2 years of relevant experience in the pharmaceutical industry. Freshers are highly encouraged to apply.
- Core Skills: Ability to learn machine operation, maintain production standards, and follow safety protocols.
2. QC Analyst (Quality Control – Transdermal)
As a QC Analyst, you will play a vital role in ensuring that our pharmaceutical products meet rigorous quality and safety benchmarks. We are looking for experienced professionals who are proficient in advanced analytical techniques.
- Qualifications: B.Sc, M.Sc, or B. Pharm.
- Experience: 4 to 8 years of hands-on experience in the pharmaceutical industry.
- Core Skills: Deep technical proficiency in HPLC, GC, KF, UV, FTIR, and LIMS. You must have a strong background in analytical testing and documentation.
3. GLP Analyst (Quality Control – Transdermal)
The GLP (Good Laboratory Practice) Analyst position is responsible for maintaining high standards of laboratory operations, including instrument management and compliance. This role requires a strong understanding of regulatory requirements and chemical laboratory operations.
- Qualifications: B.Sc, M.Sc, or B. Pharm.
- Experience: 4 to 8 years of direct experience in the pharmaceutical sector.
- Core Skills: Extensive knowledge of instrument calibration and qualification, working standards qualification, chemical procurement, and CSVMP of QC instruments. Proficiency in LIMS and SAP software is essential for this role.
Interview Details
We invite all eligible candidates to attend our upcoming walk-in interview. Please ensure you bring your updated resume, academic certificates, and proof of prior work experience.
- Date: 21st March 2026
- Time: 9:00 AM to 3:00 PM
- Venue: Zydus Lifesciences Limited, Plot No. 1/B, Pharmez – SEZ, Special Economic Zone, NH-8A, Matoda, Sanand, Ahmedabad – 382213, India.
Why Work With Us?
At Zydus Lifesciences, we believe that our employees are our most valuable asset. We provide a collaborative work environment that fosters professional growth and innovation. Whether you are a fresh graduate looking for your first break or an experienced professional looking to advance your career, we offer a challenging and rewarding workplace where you can make a genuine impact on global health.
Application Instructions
This is a walk-in recruitment process. Candidates are requested to arrive at the venue within the specified time frame. Please ensure that you carry a copy of your CV, recent passport-sized photographs, and relevant ID proofs.
Our team will conduct on-the-spot interviews and assessments for qualified candidates. We look forward to meeting passionate individuals who are ready to contribute to our mission of providing high-quality pharmaceutical products.
Important Note: Candidates are advised to adhere to the company’s dress code and safety guidelines upon arrival at the facility. Please ensure all your documentation is organized and ready for review during the interview process.